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. Author manuscript; available in PMC: 2010 Apr 1.
Published in final edited form as: Bone Marrow Transplant. 2009 Mar 23;44(7):441–447. doi: 10.1038/bmt.2009.56

Table 1. Baseline and demographic factors in cases with severe hepatocellular injury and concurrent controls.

Cases
(n=88)
Controls
(n=6137)
p-value
Age at transplant 0.9764
 Mean ± SD 40.6 ± 15.8 40.4 ± 17.1
 Median (range) 45.3 (2 - 68) 43.3 (0 - 78)
Male patients 52 (59.0%) 3433 (55.9%) 0.5898
Primary diagnosis 0.4805
 Hematologic malignancies (non-lymphoma) 48 (54.5%) 3165 (51.6%)
 Lymphoma 17 (19.3%) 1027 (16.7%)
 Other malignancy 17 (19.3%) 1616 (26.3%)
 Other than malignancy 6 (6.8%) 328 (5.3%)
Second or more HCT 10 (11.4%) 594 (9.7%) 0.5848
Allogeneic transplant 62 (70.5%) 4328 (70.5%) 1.000
Source of donor cells (allogeneic HCT only) 0.3713
 Peripheral blood stem cells 31 (50%) 1940 (45%)
 Bone marrow 31 (50%) 2388 (55%)
Other than HLA identical sibling donor (allogeneic HCT only) 35 (56.5%) 2487 (57.5%) 0.8975
Conditioning regimen
 Myeloablative regimen1 81 (92.0%) 5395 (87.9%) 0.1835
 Reduced intensity regimen 7 (8.0%) 742 (12.1%)
Positive CMV serostatus at transplant (donor or recipient) 48 (54.6%) 3940 (64.5%) 0.0570
Ursodiol prophylaxis 19 (21.6%) 1661 (27.1%) 0.2779
1

Includes regimens received by 3 patients whose severe hepatocellular injury occurred later, following infusion of gemtuzumab ozogamicin for treatment of recurrent leukemia after transplant.18